(Q42478287)

1 November 2017

title

Defective glycosylation of α-dystroglycan contributes to podocyte flattening (English)

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1 November 2017

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Kenichiro Kojima

1

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1 November 2017

Hitonari Nosaka

2

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1 November 2017

Yuki Kishimoto

3

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1 November 2017

Yuri Nishiyama

4

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1 November 2017

Seiichi Fukuda

5

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1 November 2017

Masaru Shimada

6

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1 November 2017

Kenzo Kodaka

7

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1 November 2017

Fumiaki Saito

8

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1 November 2017

Kiichiro Matsumura

9

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1 November 2017

Teruo Shimizu

10

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1 November 2017

Tatsushi Toda

11

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1 November 2017

Satoshi Takeda

12

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1 November 2017

Hiroshi Kawachi

13

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1 November 2017

Shunya Uchida

14

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1 November 2017

language of work or name

English

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publication date

13 October 2010

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1 November 2017

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1 November 2017

volume

79

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1 November 2017

issue

3

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1 November 2017

page(s)

311-316

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Caught flat-footed: podocyte damage and the molecular bases of focal glomerulosclerosis

1 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Podocyte injury and targeting therapy: an update

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Protection of alpha(3) integrin-mediated podocyte shape by superoxide dismutase in the puromycin aminonucleoside nephrosis rat.

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Expression of agrin, dystroglycan, and utrophin in normal renal tissue and in experimental glomerulopathies

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Nephrin is specifically located at the slit diaphragm of glomerular podocytes

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Dystroglycan versatility

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Dystroglycan in development and disease.

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

The crystal structure of a laminin G-like module reveals the molecular basis of alpha-dystroglycan binding to laminins, perlecan, and agrin

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Podocyte flattening and disorder of glomerular basement membrane are associated with splitting of dystroglycan-matrix interaction

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Reactive oxygen species deglycosilate glomerular alpha-dystroglycan.

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Glomerular epithelial alterations resulting from sialic acid surface coat removal

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Loss of heparan sulfate glycosaminoglycan assembly in podocytes does not lead to proteinuria

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Nephrin redistribution on podocytes is a potential mechanism for proteinuria in patients with primary acquired nephrotic syndrome

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Basement membrane fragility underlies embryonic lethality in fukutin-null mice

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Laminin polymerization induces a receptor-cytoskeleton network

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Cloning of rat nephrin: expression in developing glomeruli and in proteinuric states

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https://api.crossref.org/works/10.1038%2FKI.2010.403

7 January 2021

Identifiers

DOI

10.1038/KI.2010.403

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1 November 2017

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